NDC 68788-8358 – Divalproex sodium

Divalproex Sodium 500 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC68788-8358

Product details

Brand name
Divalproex sodium
Generic name
Divalproex sodium
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA209286
Marketed since
February 13, 2023
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent; Mood Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Divalproex Sodium →

Package NDC codes (3)

Package NDCDescriptionSince
68788-8358-330 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-3)Feb 13, 2023
68788-8358-660 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-6)Feb 13, 2023
68788-8358-990 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-9)Feb 13, 2023

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